A citation-based method for searching scientific literature

Takeshi Tokuyama, Asei Hirai, Isshin Shiiba, Naoki Ito, Keigo Matsuno, Keisuke Takeda, Kanata Saito, Koki Mii, Nobuko Matsushita, Toshifumi Fukuda, Ryoko Inatome, Shigeru Yanagi. Biomolecules 2020
Times Cited: 5







List of co-cited articles
3 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity



MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options.
Ayman W El-Hattab, Adekunle M Adesina, Jeremy Jones, Fernando Scaglia. Mol Genet Metab 2015
212
40

Mitochondrial dynamics: overview of molecular mechanisms.
Lisa Tilokani, Shun Nagashima, Vincent Paupe, Julien Prudent. Essays Biochem 2018
281
40


Biomarkers in rare neuromuscular diseases.
Chiara Scotton, Chiara Passarelli, Marcella Neri, Alessandra Ferlini. Exp Cell Res 2014
17
20

Mitochondrial control of the NLRP3 inflammasome.
Oliver Kepp, Lorenzo Galluzzi, Guido Kroemer. Nat Immunol 2011
104
20

A valid mouse model of AGRIN-associated congenital myasthenic syndrome.
Laurent P Bogdanik, Robert W Burgess. Hum Mol Genet 2011
33
20

The Relevance of Oxidative Stress in the Pathogenesis and Therapy of Retinal Dystrophies.
Elena B Domènech, Gemma Marfany. Antioxidants (Basel) 2020
32
20

Peripheral neuropathy in mitochondrial disease.
G Pezeshkpour, C Krarup, F Buchthal, S DiMauro, N Bresolin, J McBurney. J Neurol Sci 1987
59
20

Mitochondrial homeostasis: the interplay between mitophagy and mitochondrial biogenesis.
Konstantinos Palikaras, Nektarios Tavernarakis. Exp Gerontol 2014
199
20

Loss of the autophagy protein Atg16L1 enhances endotoxin-induced IL-1beta production.
Tatsuya Saitoh, Naonobu Fujita, Myoung Ho Jang, Satoshi Uematsu, Bo-Gie Yang, Takashi Satoh, Hiroko Omori, Takeshi Noda, Naoki Yamamoto, Masaaki Komatsu,[...]. Nature 2008
20

Emery-Dreifuss muscular dystrophy.
Megan Puckelwartz, Elizabeth M McNally. Handb Clin Neurol 2011
31
20

AMPK activation stimulates autophagy and ameliorates muscular dystrophy in the mdx mouse diaphragm.
Marion Pauly, Frederic Daussin, Yan Burelle, Tong Li, Richard Godin, Jeremy Fauconnier, Christelle Koechlin-Ramonatxo, Gerald Hugon, Alain Lacampagne, Marjorie Coisy-Quivy,[...]. Am J Pathol 2012
145
20

Mitochondrial DNA mutations in neurodegeneration.
Michael J Keogh, Patrick F Chinnery. Biochim Biophys Acta 2015
70
20

The 2018 version of the gene table of monogenic neuromuscular disorders (nuclear genome).
Gisèle Bonne, François Rivier, Dalil Hamroun. Neuromuscul Disord 2017
20
20

Genetic Modifiers for Neuromuscular Diseases.
Kay-Marie Lamar, Elizabeth M McNally. J Neuromuscul Dis 2014
16
20

The excitation-contraction coupling mechanism in skeletal muscle.
Juan C Calderón, Pura Bolaños, Carlo Caputo. Biophys Rev 2014
47
20


Association of a Novel ACTA1 Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended Family.
Kristen Zukosky, Katherine Meilleur, Bryan J Traynor, Jahannaz Dastgir, Livija Medne, Marcella Devoto, James Collins, Jachinta Rooney, Yaqun Zou, Michele L Yang,[...]. JAMA Neurol 2015
24
20

Up-regulation of Toll-like receptors 7 and 9 and its potential implications in the pathogenic mechanisms of LMNA-related myopathies.
Cristina Cappelletti, Franco Salerno, Eleonora Canioni, Marina Mora, Renato Mantegazza, Pia Bernasconi, Lorenzo Maggi. Nucleus 2018
7
20

Mitophagy is triggered by mild oxidative stress in a mitochondrial fission dependent manner.
Magdalena Frank, Stéphane Duvezin-Caubet, Sebastian Koob, Angelo Occhipinti, Ravi Jagasia, Anton Petcherski, Mika O Ruonala, Muriel Priault, Bénédicte Salin, Andreas S Reichert. Biochim Biophys Acta 2012
279
20

Hyperthyroid myopathy with mitochondrial paracrystalline rectangular inclusions.
J Lloreta, J Roquer, J M Corominas, S Serrano. Ultrastruct Pathol 1996
10
20

A unifying genetic model for facioscapulohumeral muscular dystrophy.
Richard J L F Lemmers, Patrick J van der Vliet, Rinse Klooster, Sabrina Sacconi, Pilar Camaño, Johannes G Dauwerse, Lauren Snider, Kirsten R Straasheijm, Gert Jan van Ommen, George W Padberg,[...]. Science 2010
434
20

Autophagy proteins regulate innate immune responses by inhibiting the release of mitochondrial DNA mediated by the NALP3 inflammasome.
Kiichi Nakahira, Jeffrey Adam Haspel, Vijay A K Rathinam, Seon-Jin Lee, Tamas Dolinay, Hilaire C Lam, Joshua A Englert, Marlene Rabinovitch, Manuela Cernadas, Hong Pyo Kim,[...]. Nat Immunol 2011
20

Safety, tolerability, and preliminary efficacy of an IGF-1 mimetic in patients with spinal and bulbar muscular atrophy: a randomised, placebo-controlled trial.
Christopher Grunseich, Ram Miller, Therese Swan, David J Glass, Mohamed El Mouelhi, Mara Fornaro, Olivier Petricoul, Igor Vostiar, Ronenn Roubenoff, Matthew N Meriggioli,[...]. Lancet Neurol 2018
14
20

Autophagy is defective in collagen VI muscular dystrophies, and its reactivation rescues myofiber degeneration.
Paolo Grumati, Luisa Coletto, Patrizia Sabatelli, Matilde Cescon, Alessia Angelin, Enrico Bertaggia, Bert Blaauw, Anna Urciuolo, Tania Tiepolo, Luciano Merlini,[...]. Nat Med 2010
356
20

Mutations of optineurin in amyotrophic lateral sclerosis.
Hirofumi Maruyama, Hiroyuki Morino, Hidefumi Ito, Yuishin Izumi, Hidemasa Kato, Yasuhito Watanabe, Yoshimi Kinoshita, Masaki Kamada, Hiroyuki Nodera, Hidenori Suzuki,[...]. Nature 2010
826
20

Genetic approaches to the treatment of inherited neuromuscular diseases.
Bhavya Ravi, Anthony Antonellis, Charlotte J Sumner, Andrew P Lieberman. Hum Mol Genet 2019
10
20

Synchronized mitochondrial and cytosolic translation programs.
Mary T Couvillion, Iliana C Soto, Gergana Shipkovenska, L Stirling Churchman. Nature 2016
144
20

Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation.
Ronen Spiegel, Ann Saada, Padraig J Flannery, Florence Burté, Devorah Soiferman, Morad Khayat, Verónica Eisner, Eugene Vladovski, Robert W Taylor, Laurence A Bindoff,[...]. J Med Genet 2016
54
20

Mitochondrial dysfunction and the inflammatory response.
María J López-Armada, Romina R Riveiro-Naveira, Carlos Vaamonde-García, Marta N Valcárcel-Ares. Mitochondrion 2013
226
20

Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase.
John Mitchell, Praveen Paul, Han-Jou Chen, Alex Morris, Miles Payling, Mario Falchi, James Habgood, Stefania Panoutsou, Sabine Winkler, Veronica Tisato,[...]. Proc Natl Acad Sci U S A 2010
165
20

Mitochondrial dysfunction in myofibrillar myopathy.
Amy E Vincent, John P Grady, Mariana C Rocha, Charlotte L Alston, Karolina A Rygiel, Rita Barresi, Robert W Taylor, Doug M Turnbull. Neuromuscul Disord 2016
20
20

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.
Stephan Züchner, Irina V Mersiyanova, Maria Muglia, Nisrine Bissar-Tadmouri, Julie Rochelle, Elena L Dadali, Mario Zappia, Eva Nelis, Alessandra Patitucci, Jan Senderek,[...]. Nat Genet 2004
20

Mitochondrial DNA depletion in sporadic inclusion body myositis.
Padmanabh S Bhatt, Charalampos Tzoulis, Novin Balafkan, Hrvoje Miletic, Gia Tuong Thi Tran, Petter Schandl Sanaker, Laurence A Bindoff. Neuromuscul Disord 2019
4
25

A novel FLNC frameshift and an OBSCN variant in a family with distal muscular dystrophy.
Daniela Rossi, Johanna Palmio, Anni Evilä, Lucia Galli, Virginia Barone, Tracy A Caldwell, Rachel A Policke, Esraa Aldkheil, Christopher E Berndsen, Nathan T Wright,[...]. PLoS One 2017
21
20

CRISPR for Neuromuscular Disorders: Gene Editing and Beyond.
Courtney S Young, April D Pyle, Melissa J Spencer. Physiology (Bethesda) 2019
9
20

Measuring In Vivo Mitophagy.
Nuo Sun, Jeanho Yun, Jie Liu, Daniela Malide, Chengyu Liu, Ilsa I Rovira, Kira M Holmström, Maria M Fergusson, Young Hyun Yoo, Christian A Combs,[...]. Mol Cell 2015
303
20



Relationships Between Ion Channels, Mitochondrial Functions and Inflammation in Human Aging.
Marie Strickland, Besma Yacoubi-Loueslati, Balkiss Bouhaouala-Zahar, Sylvia L F Pender, Anis Larbi. Front Physiol 2019
17
20

Comparative transcriptional pathway bioinformatic analysis of dietary restriction, Sir2, p53 and resveratrol life span extension in Drosophila.
Michael Antosh, Rachel Whitaker, Adam Kroll, Suzanne Hosier, Chengyi Chang, Johannes Bauer, Leon Cooper, Nicola Neretti, Stephen L Helfand. Cell Cycle 2011
25
20

Mitochondrial dysfunction and neuromuscular disease.
R A Nardin, D R Johns. Muscle Nerve 2001
61
20

An analysis of original research contributions toward FDA-approved drugs.
Eric V Patridge, Peter C Gareiss, Michael S Kinch, Denton W Hoyer. Drug Discov Today 2015
16
20


Mitochondrial DNA disturbances and deregulated expression of oxidative phosphorylation and mitochondrial fusion proteins in sporadic inclusion body myositis.
Marc Catalán-García, Glòria Garrabou, Constanza Morén, Mariona Guitart-Mampel, Adriana Hernando, Àngels Díaz-Ramos, Ingrid González-Casacuberta, Diana-Luz Juárez, Maria Bañó, Jennifer Enrich-Bengoa,[...]. Clin Sci (Lond) 2016
22
20

The ubiquitin kinase PINK1 recruits autophagy receptors to induce mitophagy.
Michael Lazarou, Danielle A Sliter, Lesley A Kane, Shireen A Sarraf, Chunxin Wang, Jonathon L Burman, Dionisia P Sideris, Adam I Fogel, Richard J Youle. Nature 2015
20

Historical landmarks of autophagy research.
Yoshinori Ohsumi. Cell Res 2014
498
20

Polyglutamine androgen receptor-mediated neuromuscular disease.
Elisa Giorgetti, Andrew P Lieberman. Cell Mol Life Sci 2016
17
20

Mechanisms and functions of inflammasomes.
Mohamed Lamkanfi, Vishva M Dixit. Cell 2014
20


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.